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首页> 外文期刊>The Analyst: The Analytical Journal of the Royal Society of Chemistry: A Monthly International Publication Dealing with All Branches of Analytical Chemistry >Amperometric immunosensor based on gold nanoparticles/alumina sol–gel modified screen-printed electrodes for antibodies to Plasmodium falciparum histidine rich protein-2
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Amperometric immunosensor based on gold nanoparticles/alumina sol–gel modified screen-printed electrodes for antibodies to Plasmodium falciparum histidine rich protein-2

机译:基于金纳米颗粒/氧化铝溶胶-凝胶修饰的丝网印刷电极的安培免疫传感器,用于抗恶性疟原虫组氨酸富集蛋白2的抗体

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摘要

We report herein the amperometric immunosensor for antibodies to Plasmodium falciparum histidine rich protein-2 (PfHRP-2). Screen-printed electrodes (SPEs) were modified with alumina sol–gel (Al2O3 sol–gel) derived film and gold nanoparticles i.e. AuNPs/Al2O3sol–gel/SPE. A thin film was formed by dripping Al2O3 sol on SPE followed by electrochemical deposition of gold nanoparticles (AuNPs). The modified SPEs were characterized by scanning electron microscopy/energy dispersive X-ray analysis (SEM-EDAX), Raman spectra and voltammetric experiments. Antibodies in rabbit serum sample were allowed to react with the PfHRP-2 protein that was immobilized on the modified SPE to form antigenantibody immune complex (PfHRP-2/anti-PfHRP-2). The bound antibodies were quantified by alkaline phosphatase (AP) enzyme labeled secondary antibodies (anti-rabbit immunoglobulins-AP conjugate). Enzymatic substrate, 1-naphthyl phosphate was converted to 1-naphthol by AP and an electroactive product was quantified using amperometry. The performances of the developed immunosensor and Dot-ELISA were tested against different dilutions of hyper immune serum (rabbit anti-PfHRP-2). Dot ELISA and the developed immunosensor (AuNPs/Al2O3sol–gel/SPE) results for the hyper immune serum containing anti-PfHRP-2 were distinctly positive when diluted upto 8 times (1 : 12800 dilution) and 11 times (1 : 102400 dilution), respectively. The developed immunosensor was applied for antibodies to PfHRP-2 in human clinical samples.
机译:我们在此报告了针对恶性疟原虫组氨酸富蛋白-2(PfHRP-2)抗体的安培免疫传感器。用氧化铝溶胶-凝胶(Al2O3溶胶-凝胶)衍生的膜和金纳米颗粒(即AuNPs / Al2O3sol-gel / SPE)修饰丝网印刷电极(SPE)。通过在SPE上滴加Al2O3溶胶,然后电化学沉积金纳米颗粒(AuNPs)形成薄膜。通过扫描电子显微镜/能量色散X射线分析(SEM-EDAX),拉曼光谱和伏安实验对改性SPE进行了表征。使兔血清样品中的抗体与固定在修饰的SPE上的PfHRP-2蛋白反应,形成抗原抗体免疫复合物(PfHRP-2 / anti-PfHRP-2)。结合的抗体通过碱性磷酸酶(AP)酶标记的第二抗体(抗兔免疫球蛋白-AP偶联物)进行定量。通过AP将酶促底物磷酸1-萘酯转化为1-萘酚,并使用安培法对电活性产物进行定量。针对不同稀释度的高免疫血清(兔抗PfHRP-2),测试了开发的免疫传感器和Dot-ELISA的性能。当分别稀释至8倍(1:12800稀释度)和11倍(1:102400稀释度)时,包含抗PfHRP-2的超免疫血清的点ELISA和已开发的免疫传感器(AuNPs / Al2O3sol-gel / SPE)结果明显为阳性。 , 分别。研发的免疫传感器用于人类临床样品中针对PfHRP-2的抗体。

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